Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Motiva Implants® Post-Approval Study
NCT06938399 · View on ClinicalTrials.gov ↗
Study Summary
This study examines the general post-market use and safety of Motiva Implants® and gathers and assesses selected safety and effectiveness data about their post market performance and experience.
Conditions Studied
Interventions
- DEVICE Silicone gel-filled breast implants - Motiva Implants®
- OTHER Aesthetic Surgery
Study Locations (20)
California
- J. Gerald Minniti, M.D., F.A.C.S. — Beverly Hills
- AESTHETX Center — Camp Pendleton
- Align Surgical Associates Inc — San Francisco
- Schwartz Aesthetic Institute — Westlake Village
New Jersey
- Delaware Valley Plastic Surgery — Cherry Hill
- Caroline A. Glicksman MD — Sea Girt
New York
- Mark D. Epstein, MD, FACS Center for Aesthetic Surgery — Hauppauge
- Neinstein Plastic Surgery — New York
North Carolina
- HKB Cosmetic Surgery — Charlotte
- Capizzi, MD Cosmetic Surgery & Med Spa — Charlotte
Texas
- Restora Austin Plastic Surgery Center — Austin
- Austin Plastic Surgeon — Austin
Colorado
- The Center for Cosmetic Surgery — Denver
District of Columbia
- Advanced Plastic Surgery, LLC — Washington D.C.
Florida
- Careaga Plastic Surgery — Coral Gables
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,400 participants |
| Start Date | 2025-05-01 |
| Est. Completion | 2037-07-31 |
| Phase | NA |
Interested in This Trial?
Always speak with your doctor before enrolling in a clinical trial.
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06938399
The ClinicalTrials.gov registry entry for NCT06938399 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 2,400 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Motiva USA, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Breast Implant appearing as the primary indexed condition, and to 2 interventions — of which Silicone gel-filled breast implants - Motiva Implants® is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06938399 reports 20 study locations spanning 13 distinct geographic areas — top geographies include California, New Jersey, New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06938399 about?
NCT06938399 is a clinical study titled "Motiva Implants® Post-Approval Study". This study examines the general post-market use and safety of Motiva Implants® and gathers and assesses selected safety and effectiveness data about their post market performance and experience.
What is the current status of trial NCT06938399?
This trial is currently recruiting. It is a NA study. The enrollment target is 2,400 participants. The study started on 2025-05-01. Estimated completion is 2037-07-31.
What conditions does trial NCT06938399 study?
This clinical trial studies the following conditions: Breast Implant. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06938399?
The interventions under investigation include: Silicone gel-filled breast implants - Motiva Implants® (DEVICE), Aesthetic Surgery (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06938399?
This trial is sponsored by Motiva USA, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06938399 being conducted?
This trial has 20 study locations across California, Colorado, District of Columbia, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How Clinical Trials Work
Understand phases 1-4, trial design, randomization, and the informed consent process.
Patient Rights in Clinical Trials
Your rights as a participant: consent, withdrawal, privacy, and who to contact.
Finding the Right Clinical Trial
A practical guide to searching trials, understanding eligibility, and evaluating options.
All Guides
Browse our complete library of clinical trial educational resources.
Read our methodology — how this data is sourced, computed, and verified.